Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_provenance.
- NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_assertion description "[A patient with a rare leukodystrophy related to lamin B1 duplication.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_provenance.
- NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_assertion evidence source_evidence_literature NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_provenance.
- NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_assertion SIO_000772 22973660 NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_provenance.
- NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_assertion wasDerivedFrom befree-20150227 NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_provenance.
- NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_assertion wasGeneratedBy ECO_0000203 NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP537941.RAG_82HQkVQ8FF2aRMU21BQWvN-NZ5H7Xnu1rLhBs2iGc130_provenance.